drugset / Trial / NCT06450639

A Study to Assess the Efficacy and Safety of Satralizumab in Duchenne Muscular Dystrophy (DMD)

NCT06450639

Phase 2 Active not recruiting 30 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the efficacy, safety, pharmacokinetics (PK) and pharmacodynamics (PD) of satralizumab, a humanized anti-interleukin-6 receptor (aIL-6R) monoclonal antibody, in ambulatory and non-ambulatory participants with DMD aged ≥ 8 to \< 18 years old receiving corticosteroid therapy.

Timeline

Start
2025-04-04
Primary completion
2026-08-26
Completion
2026-11-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Satralizumab Monoclonal antibody Subcutaneous